Research & Development

Advance your expertise in R&D. We prepare you for the challenges across all clinical and non-clinical areas in your work with small molecules and biologics.

Thema
Dates
Format

Mastering ICH Quality Guidelines: From Development to Lifecycle Management

To make the most of ICH Q12 opportunities, you have to be aware of the relation between ICH guidelines Q8 to Q12 and how to properly integrate them. Our experts will go through each guideline and…
Language: English
18/11/2026
Online-Seminar
Details

Preclinical development: From bench to first in human

Preclinical drug development: The online training course for preclinical newcomers with a focus on small molecules and biologics. Learn about the fundamentals and regulatory requirements and take the…
Language: English
01 - 03/12/2026
Online-Seminar
Details

AI in Pharma R&D

AI in Pharma R&D: During the half-day seminar you will learn how to navigate compliance requirements due to regulatory frameworks, you will explore how structured content enables AI-supported document…
Language: English
17/11/2026
Online-Seminar
Details

e-Learning: Global Stability

Global Stability: This e-Learning provides a comprehensive introduction to global stability testing for pharmaceutical products (chemical and biological products). Including an update on revision of…
Language: English
available immediately
e-Learning
Details

Biopharmaceuticals

The compact course with a content focus on the development, production and analytics of biotech drugs. Secure your place and qualify now! All three course days can be booked individually (single day =…
Language: English
02 - 04/12/2026
Online-Seminar
Details

EU Biotech Act: What Pharma R&D Professionals need to know

The EU Biotech Act is still evolving - but preparation cannot wait. Join experts from authority and industry to understand what is coming, what remains uncertain, and how to get your R&D…
Language: English
17/11/2026
Online-Seminar
Details

Update: Method validation & analytical methods transfer

Master GMP-compliant method validation and analytical method transfer in one focused online seminar. Walk away with practical knowledge of current ICH and FDA requirements, solid statistical…
Language: English
18/11/2026
Online-Seminar
Details

Global stability: From regulatory framework to practical application

Navigate global stability requirements with confidence - from ICH, FDA and EMA frameworks to real-world application. In this interactive half-day seminar, you work through practical case studies,…
Language: English
26/11/2026
Online-Seminar
Details

Toxicology and beyond: Safety assessment in drug development

During our online training "Toxicology and beyond: Safety assessment in drug development" you will build a solid toxicological know-how basis and will be informed about the inclusion of toxicological…
Language: English
28 - 29/09/2026
Online-Seminar
Details

CTD: requirements for non-clinical/clinical modules and eCTD-readiness

Non-clinical/clinical content in the dossier: Are you a beginner in the field and would like to feel confident working competently on modules 2, 4 and 5 in the future? Are you already an experienced…
Language: English
21 - 22/09/2026
Online-Seminar
Details

Contact

We are happy to provide you with personal and individual advice.

Our professional development portfolio is extensive. We would be pleased to discuss your requirements with you personally and help identify the most suitable options from our range of offerings. Let our professional development experts advise you and feel free to contact us today.

Dr. Birgit Wessels
Conference Manager Healthcare
+49 6221 500-652
b.wessels@forum-institut.de